Robots offer clues to the impressive robustness of eel locomotion
Peer-Reviewed Publication
Updates every hour. Last Updated: 21-Sep-2025 22:11 ET (22-Sep-2025 02:11 GMT/UTC)
Researchers have discovered that reef-building corals use chloride ions, rather than amino acids, to absorb visible light in their light-sensing proteins, called opsins. This unique mechanism allows opsins to switch between UV and visible light sensitivity in a pH-dependent manner, revealing new insights into coral biology and the evolution of animal vision.
Organic–inorganic hybrid perovskite solar cells achieve remarkable efficiencies (> 26%) yet face stability challenges. Quasi-2D alternating-cation-interlayer perovskites offer enhanced stability through hydrophobic spacer cations but suffer from vertical phase segregation and buried interface defects. Herein, we introduce dicyanodiamide (DCD) to simultaneously address these dual limitations in GA(MA)nPbnI3n+1 perovskites. The guanidine group in DCD passivates undercoordinated Pb2+ and MA+ vacancies at the perovskite/TiO2 interface, while cyano groups eliminate oxygen vacancies in TiO2 via Ti4+–CN coordination, reducing interfacial trap density by 73% with respect to the control sample. In addition, DCD regulates crystallization kinetics, suppressing low-n-phase aggregation and promoting vertical alignment of high-n phases, which benefit for carrier transport. This dual-functional modification enhances charge transport and stabilizes energy-level alignment. The optimized devices achieve a record power conversion efficiency of 21.54% (vs. 19.05% control) and retain 94% initial efficiency after 1200 h, outperforming unmodified counterparts (84% retention). Combining defect passivation with phase homogenization, this work establishes a molecular bridge strategy to decouple stability-efficiency trade-offs in low-dimensional perovskites, providing a universal framework for interface engineering in high-performance optoelectronics.
A new species of a native bushland marsupial – closely related to the kangaroo – has been discovered but is already likely extinct, new research shows.
The humble rodent “thumb” may not seem like an obvious window into evolution, but its keratinized tip – the unguis (hoof, claw, or nail) – turns out to reveal striking insights into rodent history and adaptation, according to a new study. The findings suggest that rodents owe much of their evolutionary success to their thumb-nail (the first digit, D1), an adaptation that gave them dexterous hands for cracking seeds and nuts. The tetrapod (four-limbed vertebrate) hand is a crucial structure for interacting with the environment, and its digits show great evolutionary diversity in both form and function. Among them, the first digit – D1 – is especially intriguing: it is the last to appear during development, the first to be reduced or lost in evolution, and in some lineages, like primates, it has enabled dexterous behaviors, such as grasping or climbing. Yet, the unguis has rarely been studied in detail. In rodents, the most speciose group of mammals, the D1 may bear a nail, a claw, or no unguis at all, but the evolutionary patterns and functional significance of this variation remain poorly understood.
Here, Rafaela Missagia and colleagues use advanced phylogenetic comparative methods to systematically examine the diversity, evolutionary history, and behavioral correlates of the D1 ungis types across Rodentia. Missagia et al. found that a nail, rather than a claw, is both the most common and the likely ancestral condition. Fossil evidence suggests that rodents have borne nail-like D1s since at least the Oligocene, marking this feature as a longstanding hallmark of the group and a unique trait among related mammalian orders. According to the authors, the D1 nail may have coevolved with the rodent’s distinctive gnawing incisors, supporting dexterous manipulation of hard foods like nuts, which would have been a key ecological advantage during the group’s early diversification. Rodent species with D1 claws and those without a D1 unguis arose later in specialized linages, likely to support specific behaviors; claws to subterranean or burrowing lineages, and the loss of the unguis to lineages that rely more heavily on oral feeding than hand use.